Zest Antibacterial Liquid Hand Soap, Fresh Aqua Gel
FDA Label NDC 81277-013
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Sodalis Usa, Llc for the product Zest Antibacterial Liquid Hand Soap, Fresh Aqua (NDC 81277-013). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding drug facts, active ingredient, purpose, uses, warnings, when using this product, stop use and ask a doctor if, keep out of reach of children, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Active Ingredient
Benzalkonium Chloride 0.13%
Purpose
Antibacterial
Uses
for handwashing to decrease bacteria on the skin
Warnings
For external use only- hands only
When Using This Product
• avoid contact with the eyes. If contact occurs, rinse eyes with water.
Stop Use And Ask A Doctor If
• irritation or redness develops.
Keep Out Of Reach Of Children
If swallowed, get medical help or contact a Poison Control Center right away.
Directions
• wet hands
• apply to palm of hand
• scrub thoroughly
• rinse thoroughly
Inactive Ingredients:
Water, Cetrimonium Chloride, Glycerin, Cocamide MEA, Lauramidopropylamine Oxide, Sodium Chloride, PEG-120 Methyl Glucose Dioleate, Myristamidopropylamine Oxide, Citric Acid, Fragrance, Tetrasodium EDTA, Aloe Barbadensis Leaf Juice, Tocopheryl Acetate, Methylchloroisothiazolinone, Green 3, Methylisothiazolinone.
Package Labeling:
Label (Label)
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